NM_024531.4:c.916G>A

HGVS Expressions

  • NG_032872.1:g.6852G>A
  • NM_024531.4:c.916G>A
  • NP_078807.1:p.Gly306Arg
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Genomic Location

Chr8:144360408

Clinvar Clinical Significance

Pathogenic

CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Clinvar

35470

Epidemiology in the Arab World

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